NaCl

OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1[C@@H]1CN(Cc2ccccc2)C[C@H]1CO
Reaction #1166
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(C#Cc2ccc([N+](=O)[O-])s2)cc1
Reaction #1723
4-[(5-nitro-2-thienyl)ethynyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCCc1ccsc1
Reaction #1827
oil
المردود 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])([O-])O.[NH4+].[Na+]
Reaction #2022
Sodium ammonium phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCNC(=O)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2068
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(OCC)C(C)CCCCOC1CCCCO1
Reaction #2110
Diethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccccc1)C1CCN(CCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2cccnc2)CC1
Reaction #2613
title compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ncoc1C(=O)c1ccoc1
Reaction #2891
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #2901
( a )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC
Reaction #2993
intended compound
المردود 50.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(/C=C\c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC
Reaction #2994
intended compound
المردود 49.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCCCCCC(=O)NCC(=O)O
Reaction #3432
N-(7-Aminoheptanoyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P([O-])(O)O.O=P([O-])([O-])O.[Cl-].[Cl-].[K+].[K+].[Na+].[Na+].[Na+]
Reaction #4257
phosphate buffered saline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)CNC(=O)OCc1ccco1
Reaction #4529
expected product
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)C(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Reaction #4552
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4594
15
المردود 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)OC(=O)N1C[C@H](OS(C)(=O)=O)C[C@H]1C(N)=O
Reaction #5163
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5167
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@@H](OS(C)(=O)=O)CN1C(=O)OC(C)(C)C
Reaction #5168
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
الصفحة 1التالي